在生物经济中发展柞蚕产业

2009亚太国家生物经济会议《亚太生物经济项目册》中有五个蚕业项目,充分显示了我国蚕业在生物经济中的地位和发展潜力。本文引入生物经济的概念,介绍了我国柞蚕生物工程的概况,提出用工业化理念发展蚕业,要用现代信息产业改造传统蚕业,在生物经济领域突破发展柞蚕产业。     

Molecular cloning and expression analysis of a CXC chemokine gene from large yellow croaker Pseudosciaena crocea

In the present study, we report the cloning of a CXCL12 chemokine gene homologue from the large yellow croaker Pseudosciaena crocea (LycCXCL12). The complete cDNA of LycCXCL12 is 678 nucleotides (nt) encoding a protein of 97 amino acids (aa), with a putative molecular weight of 11.1 kDa. The deduced LycCXCL12 contains a 22-aa signal peptide and a 75-aa mature polypeptide, which possesses the typical arrangement of four cysteines as found in other known CXC chemokines. It shares 57-68% and 32-36% aa sequence identities to known CXCL12 chemokines in fish species and other vertebrates, respectively. The LycCXCL12 gene was constitutively expressed in all tissues examined although at different levels. Upon induction with poly(I:C) or inactivated trivalent bacterial vaccine, LycCXCL12 gene expression was significantly up-regulated in gills, liver, kidney, spleen and blood at 24 h after stimulation. Time course analysis using real-time PCR showed that LycCXCL12 gene expression reached peak level in spleen and kidney at 12 h or in gills at 24 h post-induction by poly(I:C), while its expression increased to the highest level in kidney at 24h or in gills and spleen at 48 h post-induction by bacterial vaccine, indicating that LycCXCL12 gene expression was differentially regulated by poly(I:C) and bacterial vaccine.     

亚洲地区饲料中霉菌毒素危害的真实情况

霉菌毒素是动物饲料中具有危害性的成分,它们可导致畜禽多种难以判断的综合病症.霉菌毒素通常导致动物的生产性能下降,免疫机能抑制,导致动物患病,进而通过动物的肉、奶、内脏进入人类的食品链中,危害人类的健康.对这些易受环境和气候影响的天然毒素进行常规地检查和实时监控是非常有必要的.这将有助于饲料生产企业做好控制动物体内霉菌毒素潜在问题的准备,饲料生产企业或通过选择使用正确有效的霉菌毒素吸附剂,添加到饲料中以吸附饲料中的霉菌毒素;或避免购买和使用来自问题地区的霉变饲料原料.     

High‐level exogenous trans10, cis12 conjugated linoleic acid plays an anti‐lipogenesis role in bovine mammary epithelial cells

Primary bovine mammary epithelial cells (BMECs) were treated by 0, 37.5, 75, 112.5, 150 μmol/L trans10, cis12 conjugated linoleic acid (CLA) to evaluate the effects of different level trans10, cis12 CLA on lipogenesis in BMEC. Addition of 75–150 μmol/L trans10, cis12 CLA reduced significantly the triacylglycerol (TAG) content (P < 0.05), but did not have inhibiting action on cell proliferation (P > 0.05). Treatment with 150 μmol/L trans10, cis12 CLA for 48 h resulted in a 17.1% reduction (P < 0.0001) of medium chain fatty acids (MCFA, C14 < C < C16), a 26.5% reduction (P < 0.0001) of unsaturated fatty acids (UFA) and a corresponding reduction of the mRNA abundance of acetyl coenzyme A (acetylCoA) carboxylase (ACC) (P = 0.046), fatty acid synthase (FAS) (P = 0.017) and stearoylCoA desaturase1 (SCD1) (P = 0.002). Another finding was that trans10, cis12 CLA elevated expression of diacylglycerol acyltransferase2 (DGAT2) (P = 0.020) and long chain acylCoA synthetases (ACSL) (P = 0.032). In conclusion, higher trans10, cis12 CLA, not low trans10, cis12 CLA, inhibited milk fat synthesis and changed fatty acid composition by regulating the expression of FAS, ACC, SCD1, DGAT2 and ACSL.     

Acaricidal activity of extracts of neem (Azadirachta indica) oil against the larvae of the rabbit mite Sarcoptes scabiei var. cuniculi in vitro

The acaricidal activity of the petroleum ether extract, the chloroform extract and the acetic ether extract of neem (Azadirachta indica) oil against Sarcoptes scabiei var. cuniculi larvae was tested in vitro. A complementary log-log (CLL) model was used to analyze the data of the toxicity tests. The results showed that at all test time points, the petroleum ether extract demonstrated the highest activity against the larvae of S. scabiei var. cuniculi, while the activities of the chloroform extract and the acetic ether extract were similar. The activities of both the petroleum ether extract and the chloroform extract against the larvae showed the relation of time and concentration dependent. The median lethal concentration (LC(50)) of the petroleum ether extract (1.3muL/mL) was about three times that of the chloroform extract (4.1muL/mL) at 24h post-treatment. At the concentrations of 500.0muL/mL, the median lethal time (LT(50)) of the petroleum ether extract and the chloroform extract was 8.4 and 9.6h, respectively.     

家兔胸,腹,盆腔内脏初级传入神经元的分布特点

应用辣根过氧化物酶（ＨＲＰ）法和荧光素逆行追踪法，对家兔心、肺、肝、胃、肾、子宫和膀胱的初级传入神经元分布规律进行了研究，结果表明，各内脏的初级传入神经元分布节段范围广泛，又有相对集中的节段；内脏与内脏之间的部分分布节段相互重叠，即使远距离相隔的内脏亦不例外，其中胸８￣１０节段是胸、腹、盆腔脏器共同重叠节段；各内脏的感觉均经交感和副交感两个途径传入，其中心、肺、肝、肾、子宫以交感途径占优势，胃和膀     

滨白鸡纯系及杂交组合的种群关系分析

本文采用中国科学院遗传研究所研制的Ａ、Ｂ、Ｃ三个系统１２个血型因子，分析滨白鸡七个纯系和五个杂交组合的种群关系。结果表明，１２个群体可分为五个类。第一类包括５个纯系（ＮＯ２、ＮＯ７、ＮＯ６、ＮＯ３、ＮＯ８）和２个杂交组合（５×２、７×８）．第二类包括５×６组合和ＮＯ５系。第三类是４×２组合。第四类是５×４组合。第五类是ＮＯ４系。不同类品系间遗传差异大，同一类品系间则小。实际配合力测定得到的４×２、５×４２、６×４２优秀杂交组合均有一定的理论基础。     

A cluster of two psittacosis cases among women farmers exposed to Chlamydia psittaci-infected domestic poultry in Zhejiang Province,China

A cluster of Chlamydia psittaci (C. psittaci) cases was reported in Zhejiang Province, China, 2019. This study evaluates the extent of the outbreak and determines the source of infection. Real-time PCR and sequencing of the ompA gene of C. psittaci were performed to identify the cases, the domesticated poultry and close contacts. The index patient was a 76-year-old woman with chronic vertigo, and Case 2 was a 64-year-old female farmer with herpes zoster. Both women bought psittaci-infected chickens or ducks from the same mobile street vendor and raised them for 10 days and 23 days before fever onset. There were no direct contact between the two women. C. psittaci test was positive for the two patients, one sick chicken, three healthy ducks and the vendor's chicken cage. Phylogenetic analysis showed that all seven C. psittaci positive samples carried identical ompA genotype A of C. psittaci. Of all of the patients' 148 close contacts, none tested positive for C. psittaci, or developed acute respiratory symptoms. Both patients were discharged after a 4-week hospital stay. In conclusion, the source of this cluster was the poultry infected with C. psittaci, which occasionally cause infections in farmers, but inter-human transmission seems unlikely.     

Spatiotemporal heterogeneity of PPARγ expression in porcine uteroplacenta for regulating of placental angiogenesis through VEGF-mediated signalling

Non-infectious prenatal mortality severely affects the porcine industry, with pathological placentation as a likely key reason. Previous studies have demonstrated that peroxisome proliferator-activated receptor gamma (PPARγ) deficiency causes defects in the uteroplacental vasculature and induces embryonic losses in mice. However, its role in porcine placental angiogenesis remains unclear. In the present study, PPARγ expression was investigated in porcine uteroplacental tissues at gestational day (GD) 25, GD40 and GD70 via quantitative polymerase chain reaction (qPCR), Western blot and immunohistochemistry (IHC). Moreover, the roles of PPARγ in porcine placental angiogenesis were investigated using a cell model of porcine umbilical vein endothelial cells (PUVECs) to conduct proliferation, migration and tube formation assays in vitro and a mouse xenograft model to assess capillary formation in vivo. The results showed that PPARγ was mainly located in the glandular epithelium, trophoblast, amniotic chorion epithelium and vascular endothelium, as indicated by the higher expression levels at GD25 and GD40 than at GD70 in endometrium and by higher expression levels at GD40 and GD70 than at GD25 in placenta. Moreover, PPARγ expression was significantly downregulated in placenta with dead foetus. In PUVECs, knocking out PPARγ significantly inhibited proliferation, migration and tube formation in vitro and inhibited capillary formation in mouse xenografts in vivo by blocking S-phase, promoting apoptosis and downregulating the angiogenic factors of VEGF and its receptors. Overall, the spatiotemporal heterogeneity of PPARγ expression in porcine uteroplacental tissue suggests its vital role in endometrial remodelling and placental angiogenesis, and PPARγ regulates placental angiogenesis through VEGF-mediated signalling.